Sr Manufacturing Engineering

hace 2 semanas

Alajuela, Costa Rica Abbott Laboratories A tiempo completo

**About Abbott**

Abbott is a global healthcare leader, creating breakthrough science to improve people’s health. We’re always looking towards the future, anticipating changes in medical science and technology.

**Working at Abbott**

At Abbott, you can do work that matters, grow, and learn, care for yourself and family, be your true self and live a full life. You will have access to:

- Career development with an international company where you can grow the career you dream of.
- A company recognized as a great place to work in dozens of countries around the world and named one of the most admired companies in the world by Fortune.
- A company that is recognized as one of the best big companies to work for as well as a best place to work for diversity, working mothers, female executives, and scientists.

**The Opportunity**

This position works out of our Costa Rica - Alajuela location in the Structural Heart Division. In Abbott’s our business purpose is to restore health and improve quality of life through the design and provision of device and management solutions for the treatment of structural heart disease.

As the Sr. Manufacturing Engineer (NPIs), you will develop and implement optimal, cost-effective manufacturing processes and methods in accordance with product specifications and quality standards; recommends and implements improvements to production processes, methods and controls; is also responsible for the activities related to installation and validation of production lines as well as the lifecycle management of equipment.

**What You’ll Do**
- Understands product cost components and its interactions, (direct & indirect material costs, MUV, labor, overhead). Uses product cost knowledge to identify risks and opportunities.
- Performs installation/validation activities for new or existent production lines, meeting regulatory requirements. That includes equipments, process, product and test method validations.
- Estimates validation activities cost and assures it is budgeted withing financial cycle.
- Identifies, selects, and purchases equipment/fixtures according to production requirements, due to obsolescence, redundancy or line capacity expansion.
- Able to navigate and excecute activities on manufacturing systems for example, update routers, BOM's or to generate new part numbers and ZFINs.
- Leads or supports local cross functional team activities. Support/Lead global initiatives with other functions andsites (ie, RA, R&D, QA).

**Required Qualifications**
- Bachelor’s Degree in STEM careers.
- 6+ years years of manufacturing/process development experience.
- Statistical techniques knowledge (DOE, SPC) is required.
- Computer software knowledge (Microsoft Word, Excel, Power Point).
- Willing to travel.
- Experience with continuous improvement methodologies. Such as lean manufacturing techniques, value stream mapping, or similar.
- Knowledge of FDA, GMP, and ISO guidelines is required.
- Experience leading validation plans for medical industry products and processes and leading root cause problem solving methodologies.
- Experience in project management.
- Fully Bilingual (English and Spanish)
- Shift Admin

**Preferred Qualifications**
- (3-5) + years prior experience in medical devices manufacturing.
- Performance management

Follow your career aspirations to Abbott for diverse opportunities with a company that can help you build your future and live your best life. Abbott is an Equal Opportunity Employer, committed to employee diversity.

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